Department of Gastroenterology, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, 010-8543, Japan.
Dig Dis Sci. 2013 May;58(5):1207-17. doi: 10.1007/s10620-012-2515-7. Epub 2013 Jan 10.
Transforming growth factor-β1 (TGF-β1) is one of the growth factors expressed in the gut, and has been shown to play an important role in intestinal mucosal healing. We investigated the effects of TGF-β1 on the cellular functions of intestinal epithelial cells, and also evaluated its signaling pathways in these cells.
We used the rat IEC-6 intestinal epithelial cell line for these studies. The expression of TGF-β1/Smad signaling molecules was examined. We evaluated the effect of TGF-β1 on the proliferation and differentiation by the BrdU incorporation assay and real-time PCR. We manipulated the expression levels of Smad2 and Smad3 using an adenovirus system and small interfering RNA to examine the signaling pathways. The expression of Smad2 and Smad3 along the crypt-villus axis was also examined in the murine intestine.
IEC-6 cells produced TGF-β1 and expressed functional TGF-β/Smad signaling molecules. The addition of TGF-β1 in the culture medium suppressed the proliferation and increased the expression of a differentiation marker of enterocytes, in a dose-dependent manner. The adenovirus-mediated and small interfering RNA-mediated studies clearly showed that the growth inhibitory effect and the promotion of differentiation were exerted through a Smad3-dependent and a Smad2-dependent pathway, respectively. IEC-6 cells exhibited upregulated expression of an inhibitory Smad (Smad7) as a form of negative feedback via a non-Smad pathway. Smad2 was predominantly expressed in villi, and Smad3 in crypts.
TGF-β1 regulates the cellular functions of intestinal epithelial cells through both Smad-dependent and non-Smad pathways.
转化生长因子-β1(TGF-β1)是肠道中表达的生长因子之一,已被证明在肠黏膜愈合中发挥重要作用。我们研究了 TGF-β1 对肠上皮细胞细胞功能的影响,并评估了其在这些细胞中的信号通路。
我们使用大鼠 IEC-6 肠上皮细胞系进行这些研究。检查 TGF-β1/Smad 信号分子的表达。我们通过 BrdU 掺入测定和实时 PCR 评估 TGF-β1 对增殖和分化的影响。我们使用腺病毒系统和小干扰 RNA 操纵 Smad2 和 Smad3 的表达水平,以检查信号通路。还在鼠肠中检查了 Smad2 和 Smad3 在隐窝-绒毛轴上的表达。
IEC-6 细胞产生 TGF-β1 并表达功能性 TGF-β/Smad 信号分子。培养基中添加 TGF-β1 以剂量依赖的方式抑制增殖并增加肠细胞分化标志物的表达。腺病毒介导和小干扰 RNA 介导的研究清楚地表明,生长抑制作用和促进分化分别通过 Smad3 依赖性和 Smad2 依赖性途径发挥作用。IEC-6 细胞通过非 Smad 途径表现出抑制性 Smad(Smad7)的上调表达,作为一种负反馈形式。Smad2 主要在绒毛中表达,Smad3 在隐窝中表达。
TGF-β1 通过 Smad 依赖性和非 Smad 途径调节肠上皮细胞的细胞功能。